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Monitored Natural Attenuation
Release 2: April 2007 Contaminated Land Management: Ready Reference 7 – 91
7.2.11
Classifications Natural attenuation Soil/groundwater/vapour In situ
Risk management role
Typically in pathway management, may also remove source
Process variations & synonyms In situ/ex situ Natural attenuation Enhanced natural
attenuation Intrinsic (bio)remediation
Outcome Combination of destruction, dispersal and stabilisation
OUTLINE Under certain conditions, the risk presented by subsurface contamination may decrease as a result of natural processes. Monitored natural attenuation acknowledges the existence of such processes and monitors their effects to confirm that risk is likely to decrease within a specified time scale. Risk reduction may be as a result of a decrease in contaminant concentration, volume, mobility or toxicity. Processes include dispersion, dilution, sorption, volatilisation, biodegradation, chemical or biological stabilisation, transformation or destruction of contaminants. The contaminants remain in place whilst these processes take place. MNA is not a ‘do nothing’ option; there is a need to demonstrate likely and actual effectiveness at all stages. Extensive site investigation is required to characterise: the geological and groundwater conditions; contaminant characteristics (types, distribution, concentration, mobility); and degradation potential of subsurface geochemical conditions (e.g. redox potential (Eh), pH, presence of electron acceptors). Lines of evidence are used to demonstrate natural attenuation include plume status (shrinking/ stable/expanding); geochemical concentrations (e.g. contaminants, daughter products, electron acceptors, dissolved oxygen and direct laboratory data). Long-term monitoring is required to prove efficacy of processes and warn if identified receptors are likely to be impacted. Natural attenuation can be enhanced by creation of oxygenated zones to increase area and rate of aerobic biodegradation, or by creating highly reducing conditions for halogenated organics using techniques like in situ flushing (Table 7.2.4) PRBs (Table 7.2.5) or redox amendments (Table 7.2.6). Risk management may be a combination of several of these techniques, and a zone of enhanced natural attenuation downstream in the aquifer. Natural attenuation may also be used as ‘pathway management’ in tandem with an intervention for source reduction.
STRENGTHS • Cost of site investigation & long-term
monitoring is likely to be considerably cheaper than installation & operation of many remediation options
• Potential high environmental merit due to low inputs and often transformation of contaminants into innocuous by-products
• Limited intrusive work required; site can be put to productive use
• May be used in conjunction with, or after, other remedial measures
• Can be used to manage risks from contaminants (e.g. DNAPLs) which are hard to remove
WEAKNESSES • May take long time to reach remediation goal • Requires considerable site investigation • Needs long-term monitoring (years/decades) • Subsurface conditions may change, resulting
in renewed mobility of contaminants • Potential for continued contamination and
cross-media transfer of contaminants • Heterogeneity of subsurface geological and
geochemical conditions may make site characterisation and prediction of natural attenuation difficult
• Some intermediates or by-products may be as or more toxic than the original contaminants
• Rates of attenuation may drop as natural capacities are exceeded
Monitored Natural Attenuation 7.2.11
Release 2: April 2007 7 – 92 Contaminated Land Management: Ready Reference
APPLICABLE CONTAMINANTS AND MATERIALS – Outcome: combination of destruction, dispersal and stabilisation
Halogenated volatile a PCBs ? Halogenated semivolatile
a Pesticides/herbicides e Cyanides
Non-halogenated volatile
b Org
anic
Dioxins/furans Inor
gani
c
Corrosives
Non-halogenated semivolatile ?c Volatile metals ?f Asbestos
Organic corrosives ?d Non-volatile metals ?f Oxidisers
Org
anic
Organic cyanides ? Inor
gani
c Radionuclides ?h
Mis
c
Reducers
Gravel >2 mm Sand 0.06–2 mm Silt 2–60 µm Clay <2 µm Peat ? ?g ?
Key: Usually applicable; Potentially applicable; ? May be applicable; not treatable; may worsen situation. See Tables 4.9.2 and 4.9.3 for contaminant classifications.
Notes
a. Efficacy of MNA for chlorinated solvents depends on the conditions at the site b. Primarily BTEX, also others, e.g. acetone c. Some will attenuate, e.g. phenols, methanol d. Some will attenuate, e.g. acetic acid e. Old chlorinated types resist degradation. More modern ones tend to attenuate f. Cannot be destroyed, but in some cases can be immobilised g. Contaminants tend to adsorb on to the clay matrix and be temporarily immobilised.
However, these contaminants may be released slowly, with the clay acting as a long-term source (albeit at reduced concentrations) of contamination
h. Radionuclides cannot be destroyed, but radioactivity is ultimately self-limiting, and relying on this attenuation combined with institutional controls has been used to manage land suffering from acute radiological problems
LINES OF EVIDENCE
The ‘lines of evidence’ approach is based on gathering complementary data that together establish that the processes of natural attenuation are occurring and that it will be protective of human health and the environment. Although the precise terms and details vary in general, the lines of evidence used are: 1. Documented loss of contaminant mass at the field scale (note: plume trend may not be
clear from plotting data. It may be necessary to quantify the trend using statistical methods)
2. Presence and distribution of geochemical/biochemical indicators of natural attenuation 3. Direct microbiological evidence
Monitored Natural Attenuation 7.2.11
Release 2: April 2007 Contaminated Land Management: Ready Reference 7 – 93
Dominant attenuation mechanisms for key groups of contaminants (from Environment Agency 2000)
Non-degradative attenuation mechanisms
Degradative attenuation mechanisms
Contaminant type
Examples
Met
hyla
tion
Pre
cipi
tatio
n &
cat
ion
exch
ange
Sor
ptio
n &
bin
ding
Vol
atilis
atio
n
Aer
obic
deg
rada
tion
(con
tam
inan
t as
elec
tron
dono
r)
Ana
erob
ic d
egra
datio
n (c
onta
min
ant
as e
lect
ron
dono
r)
Red
uctiv
e de
halo
gena
tion
(con
tam
inan
t as
elec
tron
acce
ptor
)
Ferm
enta
tion
Co-
met
abol
ism
Oxi
datio
n/re
duct
ion
Chlorinated solvents ≥3 chlorine atoms
PCE, TCE, TCA, TCM ?
Chlorinated solvents, <3 chlorine atoms
DCM, VC, DCE
Petroleum hydrocarbons
BTEX, middle distillates
Fuel oxygenates MTBE, TAME, ETBE
Heavy metals (cationic)
Hg, Cd, Zn, Pb, Ni, Sr, Co
Heavy metals (anionic)
CrO4, AsO4, AsO3, TcO4
Inorganics Ca, Mg, Si
Anions PO4, BO3
Ammonia/ium NH3, NH4+
Cyanide CN
Nitrate NO3
PAHs Naphthalene ?
Creosote Phenols & phenolics
Pesticides Need to consider specific substance
? ?
= primary importance; = secondary importance; ? = some doubt exists over the importance of the process. NB: Dispersion and diffusion are aplicable to all contaminants and have, therefore been excluded.
Monitored Natural Attenuation 7.2.11
Release 2: April 2007 7 – 94 Contaminated Land Management: Ready Reference
EXAMPLE: BTEX NATURAL ATTENUATION (from www.howtomna.com)
Processes Biodegradation, volatilisation, sorption, dispersion and dilution (by recharge). Note: chemical degradation is insignificant
BTEX NATURAL ATTENUATION INDICATORS
Parameters Media Trend inside the plume Dissolved oxygen (DO) Groundwater Decreases Nitrate (NO3
--) Groundwater Decreases Iron (Fe3+ and Fe2+) Groundwater Fe3+ decreases as
Fe2+ increases Sulphate (SO4
2--) Groundwater Decreases Carbon dioxide (CO2) Groundwater/soil gas Increases Methane (CH4) Groundwater/soil gas Increases (in absence of oxygen)
OPERATIONAL PARAMETERS
Typical equipment Requirements for installation of monitoring wells
Operation and maintenance
Well maintenance
Monitoring progress Collection and analysis of groundwater samples
Site requirements Access; monitoring wells
Footprint Monitoring wells
Potential environmental impacts
Contamination may reach existing or new receptors before attenuation is complete. Subsurface conditions may change, affecting the progress of natural attenuation, in the worst case leading to the release of adsorbed or absorbed contaminants
Health and safety issues
Potential long-term contamination exposure of residents must be assessed at all sites
Practical depth of treatment
No limit established
Time
Dependent on the initial conditions. E.g. risk assessment may indicate that no action is required to protect downstream receptors. Modelling may indicate that after source reduction, natural attenuation will lead to effective disappearance of residual contamination over several years, with plume shrinkage evident after one year
Availability in UK Available
Monitored Natural Attenuation 7.2.11
Release 2: April 2007 Contaminated Land Management: Ready Reference 7 – 95
REFERENCES
Learning
Alvarez, P.J. and Illman, W.A. (2005) Bioremediation and Natural Attenuation: Process Fundamentals and Mathematical Models. Wiley, ISBN 0471650439. www.wiley.com
American Petroleum Institute (2003) Groundwater Remediation Strategies Tool. Regulatory and Scientific Affairs Department. Publication Number 4730. December 2003. http://api-ec.api.org//filelibrary/4730_Final.pdf
Environment Agency (1996) Evaluation of Remedial Actions for Groundwater Pollution by Organic Solvents. R&D Tech. Report P9, Bristol. ISBN 1857050525. http://publications.environment-agency.gov.uk/epages/eapublications.storefront/
Environment Agency (2004) Mobilising Nature’s Armoury: Monitored Natural Attenuation – Dealing With Pollution Using Natural Processes. Booklet SCHO0104BHTD-E-E, Environment Agency, Bristol. http://publications.environment-agency.gov.uk/epages/ eapublications. storefront/
Evans, D., Jefferis, S.A., Thomas, A.O. and Cui, S. (2001) Remedial Processes for Contaminated Land: Principles and Practice. C549. CIRIA, London. ISBN 0 86017 549 9. www.ciria.org.uk
IAEA (1999) Technologies for Remediation of Radioactively Contaminated Sites. IAEA-TECDOC-1086. IAEA, Vienna, via www.iaea.org
Land Quality Management Ltd (2001–2004) The HowToMNA website www.howtomna.com
The National Research Council (2000) Natural Attenuation for Groundwater Remediation. The National Academies Press, Washington, DC. ISBN 0309516471. http://books.nap.edu/books/0309069327/html/index.html
Sinke, A. and le Hecho, I. (1999) Monitored Natural Attenuation: Review of Existing Guidelines and Protocols. TNO-Nicole report, TNO-MEP R99/313A. TNO Institute of Environmental Sciences, Energy Research and Process Innovation, Apeldoorn. www.nicole.org
Suthersan, S.S. (1999) Remediation Engineering Design Concepts. CRC Press Inc., Boca Raton, Florida (CD-ROM). ISBN 0849321689. www.crcpress.com/
United States Department of Energy (2004) Compatibility of Alternative Chlorinated Solvent Source Treatment Strategies with Monitored Natural Attenuation – Looney, B.B. and Vangelas, K.M. http://sti.srs.gov/fulltext/ms2004236/ms2004236.pdf
United States Geological Survey (2003) Methodology for Estimating Times of Remediation Associated with Monitored Natural Attenuation – Francis H. Chapelle, Mark A. Widdowson, J. Steven Brauner, Eduardo Mendez III and Clifton C. Casey. http://toxics.usgs.gov/pubs/wri03-4057/
Water Resources Investigation Report 03-4057. http://water.usgs.gov/pubs/wri/wri034057/
Wiedemeier, T.H et al. (1999) Natural Attenuation of Fuels and Chlorinated Solvents in the Subsurface. Wiley. ISBN 0471197491. www.wiley.com
Monitored Natural Attenuation 7.2.11
Release 2: April 2007 7 – 96 Contaminated Land Management: Ready Reference
Handbooks
Air Force Center for Environmental Excellence – AFCEE (2004) Implementing Monitored Natural Attenuation and Expediting Closure at Fuel-release Sites – Brauner, J. et al. AFCEE, Brooks City-Base, Texas. NTIS: ADA426387. http://handle.dtic.mil/100.2/ADA426387
Environment Agency (2000) Guidance on the Assessment and Monitoring of Natural Attenuation of Contaminants in Groundwater – Carey, M.A., Finnamore, J.R., Morrey, M.J. and Marsland, P.A. R&D Publication 95, Environment Agency, Bristol. ISBN 1857052632. http://publications.environment-agency.gov.uk/epages/eapublications.storefront/
NOBIS (1998) Decision Support Model for Natural Attenuation, Phase 2. Report 98-1-21. CUR/NOBIS, Gouda. CUR/NOBIS, Gouda, The Netherlands. www.skbodem.nl/
United States Environmental Protection Agency (1998) Technical Protocol for Evaluating Natural Attenuation of Chlorinated Solvents in Ground Water – Wiedemeier, T.H. et al. EPA/600/R-98/128. www.cluin.org/techfocus/default.focus/sec/Natural% 5FAttenuation/cat/Guidance/ United States Environmental Protection Agency (2004) Performance Monitoring of MNA Remedies for VOCs in Ground Water. EPA 600-R-04-027. www.cluin.org/techfocus/ default.focus/sec/Natural%5FAttenuation/cat/Guidance/ United States Environmental Protection Agency (2005) Monitored Natural Attenuation of MTBE as a Risk Management Option at Leaking Underground Storage Tank Sites. EPA 600-R-04-179. www.cluin.org/techfocus/default.focus/sec/Natural%5FAttenuation/ cat/Guidance/
Case studies and demonstrations
Barr, D., Finnamore , J.R., Bardos, R.P., Weeks , J.M. and Nathanail, C.P. (2002) Biological Methods for Assessment and Remediation of Contaminated Land: Case Studies. Project RP625. CIRIA Report C575. CIRIA, London. www.ciria.org.uk Environment Agency (2003) SIReN: Phase 2B Further Investigation (Phase 2b) of the SIReN (Site for Innovative Research on Natural Attenuation) Site – Lethbridge, G., Scott, P. and Earle, R. R&D Technical Report P2-208/TR/3. Environment Agency, Bristol, UK. ISBN 1844321061. http://publications.environment-agency.gov.uk/epages/eapublications. storefront/ United States Environmental Protection Agency (2004) Performance Monitoring of MNA Remedies for VOCs in Ground Water. EPA/600/R-04/027. www.epa.gov/ada/download/ reports/600R04027/600R04027.pdf United States Environmental Protection Agency (2004) FRTR Cost and Performance Remediation Case Studies and Related Information. CD-ROM. EPA 542-C-04-004, www.frtr.gov (has a comprehensive listing of case studies), and also on www.clu-in.org
US Federal Remediation Technologies Roundtable (FRTR) Cost and performance web page: www.frtr.gov/costperf.htm